Comparison of Postoperative Analgesia Methods in Elective Cesarean Section Surgeries

Not Applicable

Completed

• Conditions: Opioid Use; Postoperative Pain

• Registration Number: NCT06425718
• Lead Sponsor: Marmara University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2024-4-26
• Last Update Posted: 2 September 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 42

Inclusion Criteria

Inclusion Criteria:<br><br> - Patients over 18 years old<br><br> - ASA II-III patients undergoing elective cesarean section<br><br>Exclusion Criteria:<br><br> - ASA IV patients<br><br> - Patients with known neurologic or psychiatric disorders<br><br> - Patients with clinically significant cardiovascular, respiratory, hepatic, renal or<br> metabolic disease<br><br> - Patients with alcohol or drug addiction<br><br> - Mentally disabled patients<br><br> - Patients with BMI>30<br><br> - Patients who develop massive bleeding or coagulopathy

Exclusion Criteria

Not provided

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Comparison of postoperative opioid consumption between two groups via Patient Controlled Analgesia (PCA) device

Secondary Outcome Measures

Name	Time	Method
Postoperative pain assessment with Numeric Rating Scale (NRS)